Position Summary:The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position will also oversee and/or perform database development and testing.Position Summary:The Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position will also oversee and/or perform database development and testing.Essential functions of the job include but are not limited to:Primary Data Management (DM) contact (Lead DM role) for assigned clinical project(s) / program(s), ensuring that there is back-up, continuity, responsiveness, and that tasks are performed in a timely manner. May support another Lead DM as a back-up and/or team member. May include DM oversight of sponsor programs.Oversee project data entry process including development of data entry guidelines, training, data entry quality and resourcingMay perform quality control of data entryProvide input, assesses and manage timelines. Ensure that clinical data management deadlines are met with quality. Assess resource needs for assigned projects, as needed.Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholdersMay assist in building clinical databasesConduct database build UAT and maintain quality controlled database build documentation. Oversee overall quality of the clinical database.May specify requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. Oversee development of the edit check specifications and manual data review specificationsResponsible for creating, revising, appropriate versioning and maintaining data management documentation. Oversee completeness of data management documentation for the Trial Master File.Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed.Review and query clinical trial data according to the Data Management PlanPerform line listing data review based on the guidance provided by the sponsor and/or Lead DMRun patient and study level status and metric reportingPerform medical coding of medical terms relative to each other in order to ensure medical logic and consistencyCoordinate SAE/AE reconciliationLiaises with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverablesMay assist with SAS programming and quality control of SAS programs used in the Data Management departmentIdentify and troubleshoot operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholdersMay assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the projectParticipate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activitiesMay attend strategy meetings, bid defense prep meetings, bid defenses, capability presentations, potential client engagement meetingsMay review Request for Proposals (RFP), proposals, provide project estimatesProvide leadership for cross-functional and organization-wide initiatives, where applicableTrains and ensures that all data management project team members have been sufficiently trainedCommunicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issuesMay present software demonstrations/trainings, department/company training sessions, present at project meetingsMay require some travelPerform other duties as assignedQualifications:Minimum Required:Bachelors and/or a combination of related experienceOther Required:8+ years' experienceProficiency in Microsoft Office: Word, Excel, PowerPoint, OutlookAble to handle a variety of clinical research tasksExcellent organizational and communication skillsProfessional use of the English language; both written and oralExperience in utilizing various clinical database management systemsBroad knowledge of drug, device and/or biologic development and effective data management practicesStrong representational skills, ability to communicate effectively orally and in writingStrong leadership and interpersonal skillsAbility to undertake occasional travelPreferred:Experience in a clinical, scientific or healthcare disciplineDictionary medical coding (MedDRA and WHODrug)Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.…)Oncology and/or Orphan Drug therapeutic experienceAny data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. 2020 Precision Medicine Group, LLCIf you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at ****** de antigüedad Intermedio#J-18808-Ljbffr
